Cleared Traditional

K971183 - GOLD FINGERS

K971183 is an FDA 510(k) clearance for GOLD FINGERS, manufactured by Alliance Rubber Products Sdn. Bhd.. The device is a Class 1 General Hospital device with product code LYY cleared through the Traditional 510(k) pathway after a 130-day FDA review.

K971183 · Alliance Rubber Products Sdn. Bhd. · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 1997
Decision
130d
Days
Class 1
Risk

K971183 is an FDA 510(k) clearance for the GOLD FINGERS. Classified as Latex Patient Examination Glove (product code LYY), Class I - General Controls.

Submitted by Alliance Rubber Products Sdn. Bhd. (Pulau Pinang, MY). The FDA issued a Cleared decision on August 8, 1997 after a review of 130 days - within the typical 510(k) review window.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6250 - the FDA general hospital device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General Hospital review framework, consistent with the majority of Class II 510(k) submissions.

View all Alliance Rubber Products Sdn. Bhd. devices

FDA 510(k) Submission Details - K971183

510(k) Number K971183 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 31, 1997
Decision Date August 08, 1997
Days to Decision 130 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
1d slower than avg
Panel avg: 129d · This submission: 130d
Pathway characteristics
Predicate-based equivalence.

LYY Device Classification - Class 1, General Controls

Product Code LYY Latex Patient Examination Glove
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.6250
Definition A Latex Patient Examination Glove Is A Disposable Device Made Of Natural Rubber Latex That May Or May Not Bear A Trace Amount Of Residual Powder, And Is Intended To Be Worn On The Hand For Medical Purposes To Provide A Barrier Against Potentially Infectious Materials And Other Contaminants.
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - LYY Latex Patient Examination Glove

All 443
Devices cleared under the same product code (LYY) and FDA review panel - the closest regulatory comparables to K971183.
W.A.
K971200 · W.A. Rubbermate Co., Ltd. · Aug 1997
DASH, SULLIVAN, VITAL GARD
K971044 · Dash Medical Gloves, Inc. · Aug 1997
POWDER FREE LATEX EXAMINATION GLOVES
K970115 · Pt Mbf Buana Multicorpora · Aug 1997
PATIENT LATEX EXAMINATION GLOVE (PREPOWDERED)
K971629 · Besglove Medicare Sdn. Bhd. · Aug 1997
UNIGLOVES
K971731 · Uni-Glove (Usa), Inc. · Aug 1997
POWDER-FREE PATIENT EXAMINATION GLOVES
K971949 · Tekmedic (M) Sdn Bhd · Jul 1997